A Randomized Controlled Trial Comparing the Incidence of Surgical Site Infections in Cesarean Sec… (NCT07395518) | Clinical Trial Compass
By InvitationNot Applicable
A Randomized Controlled Trial Comparing the Incidence of Surgical Site Infections in Cesarean Section With and Without Subcutaneous Drain Placement at Queen Savang Vadhana Memorial Hospital
Thailand86 participantsStarted 2025-06-01
Plain-language summary
To study and compare the incidence of surgical site infection after cesarean section in pregnant women with subcutaneous wound drainage and those without subcutaneous wound drainage at Queen Savang Vadhana Memorial Hospital, Sriracha. Chonburi Thailand
Who can participate
Age range18 Years
SexFEMALE
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Inclusion Criteria:
* Age ≥ 18 years
* Able to communicate in Thai
* Undergoing cesarean section, both elective and emergency procedures
* Subcutaneous fat thickness ≥ 4 cm, measured preoperatively using a standardized ultrasound technique
* Able to return for postpartum follow-up at Somdech Phra Boromrajthevi Hospital, Sriracha
* Willing to participate in the study and able to provide written informed consent
Exclusion Criteria:
* Pregnant women with chronic immunosuppressive conditions, such as systemic lupus erythematosus (SLE), HIV infection, severe anemia (Hb \< 10.0 g/dL), or uncontrolled diabetes
* Presence of skin disease or skin infection at the abdominal surgical site
* Evidence of infection prior to cesarean section
* Abnormal bleeding disorders requiring specialized treatment
* History of allergy to, or complications from, the use of wound drainage systems
* Refusal to participate in the study
What they're measuring
1
Primary outcome
Timeframe: 14 days
Trial details
NCT IDNCT07395518
SponsorQueen Savang Vadhana Memorial Hospital, Thailand